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Mutant Information

Mutant NameFN456-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN456-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 42
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr116224498C-THETINTERGENIC
SBSChr128566540A-THETINTERGENIC
SBSChr130479227A-GHETINTERGENIC
SBSChr136646900T-CHOMOUTR_3_PRIME
SBSChr140685653T-AHOMOINTERGENIC
SBSChr1016558249A-GHETSYNONYMOUS_CODING
SBSChr1019772327A-GHETINTERGENIC
SBSChr1020120036T-AHETINTERGENIC
SBSChr1022785591T-AHETINTERGENIC
SBSChr105486005T-AHOMOINTERGENIC
SBSChr1126532652T-CHETINTERGENIC
SBSChr1128344190T-GHOMONON_SYNONYMOUS_CODINGLOC_Os11g47130
SBSChr1214554936G-AHOMOINTERGENIC
SBSChr1217719998A-CHETSYNONYMOUS_CODING
SBSChr1219509480G-THOMOINTRON
SBSChr1227166873G-CHETUTR_3_PRIME
SBSChr125360423G-AHETINTERGENIC
SBSChr128954890G-THOMOINTRON
SBSChr215240744G-AHOMOINTERGENIC
SBSChr3302620T-AHOMOINTERGENIC
SBSChr334394612T-GHETSYNONYMOUS_CODING
SBSChr334885316G-AHETINTERGENIC
SBSChr410792584C-THOMOSYNONYMOUS_CODING
SBSChr412122074C-THOMOINTERGENIC
SBSChr424957348T-AHETINTERGENIC
SBSChr424957349T-AHETINTERGENIC
SBSChr425260359T-CHETINTERGENIC
SBSChr431189258T-GHETINTRON
SBSChr516500579T-CHETINTERGENIC
SBSChr517276253T-AHETINTERGENIC
SBSChr58766577C-THOMOINTERGENIC
SBSChr62646026G-AHETSTOP_GAINEDLOC_Os06g05810
SBSChr68644248A-THETINTERGENIC
SBSChr714026266C-THOMOINTERGENIC
SBSChr720823905C-THETINTERGENIC
SBSChr810987891C-AHETNON_SYNONYMOUS_CODINGLOC_Os08g17910
SBSChr812594922G-CHETINTERGENIC
SBSChr820203369A-THETINTERGENIC
SBSChr82224660G-THETNON_SYNONYMOUS_CODINGLOC_Os08g04510
SBSChr825324692C-THETINTRON
SBSChr910051383T-CHETINTRON
SBSChr92157199T-GHETSYNONYMOUS_CODING

Deletions: 31
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr21282031282041
DeletionChr4166342616634293
DeletionChr1438386743838758
DeletionChr4787092878709346
DeletionChr912089095120890972
DeletionChr912979740129797422
DeletionChr913358519133585234
DeletionChr121374400113769000250003
DeletionChr113951963139519641
DeletionChr2151582541515828531
DeletionChr816067469160674701
DeletionChr2162120421621205311
DeletionChr817218170172181788
DeletionChr1018826146188261493
DeletionChr819213259192132656
DeletionChr420574010205740111
DeletionChr320854070208540733
DeletionChr6223648712236488312LOC_Os06g37790
DeletionChr3224658352246584611
DeletionChr623016897230168981
DeletionChr224844454248444606
DeletionChr11252760012540600013000015
DeletionChr11254170012559400017700030
DeletionChr728438382284383831
DeletionChr430333426303334315
DeletionChr130932584309325895
DeletionChr131156980311569844
DeletionChr2325552873255530114
DeletionChr234973929349739334
DeletionChr235861889358618901
DeletionChr1384078383840785113

Insertions: 4
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr1225813217258132204
InsertionChr4841177584117751
InsertionChr5256768125676822
InsertionChr820502371205023711

Inversions: 5
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr1167733013216940
InversionChr11560329525593863LOC_Os11g42500
InversionChr11560353825261252LOC_Os11g42000
InversionChr664514226473547LOC_Os06g12080
InversionChr610366408147389212

Translocations: 8
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr1116229027Chr142158279
TranslocationChr1116997659Chr2474828
TranslocationChr721204845Chr68411333
TranslocationChr1223184050Chr10174004332
TranslocationChr1226150514Chr216427021LOC_Os02g27740
TranslocationChr1128162517Chr514142168LOC_Os11g46880
TranslocationChr828319003Chr55289576
TranslocationChr434006298Chr318216873LOC_Os03g31839